HGVS | Genome Assembly |
---|---|
NC_000014.9:g.50910068G= , CM000676.2:g.50910068G= | GRCh38 |
NC_000014.8:g.51376786G= , CM000676.1:g.51376786G= | GRCh37 |
NC_000014.7:g.50446536G= | NCBI36 |
NG_012796.1:g.39463C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000216392.8:c.2004C= MANE Select | ENSP00000216392.7:p.Ser668= | |
ENST00000216392.7:c.2004C= | ENSP00000216392.7:p.Ser668= | |
ENST00000532107.2:n.177C= | ||
ENST00000532462.5:c.2004C= | ENSP00000431657.1:p.Ser668= | |
ENST00000544180.6:c.1902C= | ENSP00000443787.1:p.Ser634= | |
NM_001163940.1:c.1902C= | NP_001157412.1:p.Ser634= | |
NM_002863.4:c.2004C= | NP_002854.3:p.Ser668= | |
NM_002863.5:c.2004C= MANE Select | NP_002854.3:p.Ser668= | |
NM_001163940.2:c.1902C= | NP_001157412.1:p.Ser634= |